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Associations of ghrelin with eating behaviors stress metabolic factors and telomere length among overweight and obese women: Preliminary evidence of attenuated ghrelin effects in obesity?

机译:生长激素释放肽与超重和肥胖妇女的进食行为压力代谢因子和端粒长度的关系:肥胖中生长激素释放肽作用减弱的初步证据?

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摘要

Ghrelin regulates homeostatic food intake, hedonic eating, and is a mediator in the stress response. In addition, ghrelin has metabolic, cardiovascular, and anti-aging effects. This cross-sectional study examined associations between total plasma ghrelin, caloric intake based on 3 day diet diaries, hedonic eating attitudes, stress-related and metabolic factors, and leukocyte telomere length in overweight (n=25) and obese women (n=22). We hypothesized associations between total plasma ghrelin and eating behaviors, stress, metabolic, cardiovascular, and cell aging factors among overweight women, but not among obese women due to lower circulating ghrelin levels and/or central resistance to ghrelin. Confirming previous studies demonstrating lowered plasma ghrelin in obesity, ghrelin levels were lower in the obese compared with overweight women. Among the overweight, ghrelin was positively correlated with caloric intake, giving in to cravings for highly palatable foods, and a flatter diurnal cortisol slope across 3 days. These relationships were non-significant among the obese group. Among overweight women, ghrelin was negatively correlated with insulin resistance, systolic blood pressure, and heart rate, and positively correlated with telomere length. Among the obese subjects, plasma ghrelin concentrations were negatively correlated with insulin resistance, but were not significantly correlated with blood pressure, heart rate or telomere length. Total plasma ghrelin and its associations with food intake, hedonic eating, and stress are decreased in obesity, providing evidence consistent with the theory that central resistance to ghrelin develops in obesity and ghrelin’s function in appetite regulation may have evolved to prevent starvation in food scarcity rather than cope with modern food excess. Furthermore, ghrelin is associated with metabolic and cardiovascular health, and may have anti-aging effects, but these effects may be attenuated in obesity.
机译:Ghrelin调节体内稳态食物的摄取,享乐饮食,并且是应激反应的介体。另外,生长素释放肽具有代谢,心血管和抗衰老作用。这项横断面研究检查了血浆总生长素释放肽,基于3天饮食日记的热量摄入,享乐饮食态度,压力相关和代谢因素以及超重(n = 25)和肥胖妇女(n = 22)中的白细胞端粒长度之间的关联)。我们假设超重妇女的总血浆生长素释放肽与饮食行为,压力,代谢,心血管和细胞衰老因素之间存在关联,但由于循环中的生长素释放肽水平较低和/或对生长素释放肽的中枢抗性,在肥胖女性之间没有这种关联。证实先前的研究表明肥胖症患者血浆生长素释放肽水平降低,与超重女性相比,肥胖症患者的生长激素释放肽水平较低。在超重人群中,生长素释放肽与热量摄入呈正相关,这使得人们渴望获得高度可口的食物,并且三天的昼夜皮质醇斜率更平坦。这些关系在肥胖人群中并不重要。在超重妇女中,ghrelin与胰岛素抵抗,收缩压和心率呈负相关,与端粒长度呈正相关。在肥胖受试者中,血浆生长素释放肽浓度与胰岛素抵抗呈负相关,但与血压,心率或端粒长度无显着相关。肥胖会降低血浆总生长素释放肽及其与食物摄入,享乐主义进食和压力的联系,这提供了与以下理论相一致的证据:肥胖对生长素释放肽的中央抵抗力增强,并且生长素释放肽在食欲调节中的功能可能已经发展,从而防止了食物匮乏中的饥饿而不是应付现代食物过多。此外,生长素释放肽与代谢和心血管健康有关,可能具有抗衰老作用,但肥胖会减弱这些作用。

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